Vancil Jarrod M, Henry Carolyn J, Milner Rowan J, McCoig Amber M, Lattimer Jimmy C, Villamil Jose Armando, McCaw Dudley L, Bryan Jeffrey N
Department of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.
J Am Vet Med Assoc. 2012 Jun 1;240(11):1310-5. doi: 10.2460/javma.240.11.1310.
To evaluate samarium Sm 153 lexidronam ((153)Sm-EDTMP) as a treatment option for dogs with bony tumors of the skull.
Retrospective case series.
Dogs with multilobular osteochondrosarcoma (MLO) or osteosarcoma (OSA) of the skull.
Veterinary Medical Teaching Hospital records from the Universities of Missouri and Florida from 1986 to 2006 were searched for dogs with primary skull tumors treated with (153)Sm-EDTMP.
25 dogs were initially evaluated, with 5 dogs subsequently excluded because of inadequate follow-up or unrelated death. Seven OSAs and 13 MLOs were diagnosed. Tumors involved the occipital and frontal bones (n = 10), zygomatic arch and maxilla region (6), palate (3), and mandible (1). No clinically important adverse effects related to (153)Sm-EDTMP treatment were documented. Of the 20 dogs evaluated 21 days after injection with (153)Sm-EDTMP, 4 had subjective improvement, 13 had progressive disease, and 3 had insufficient follow-up. On the basis of radiographic findings, metastasis was suspected in 1 dog; 16 dogs had no metastasis evident, and medical records were insufficient for 3 dogs. Survival time, defined as the (153)Sm-EDTMP injection date to the date of death, ranged from 3 to 1,314 days (median, 144 days).
The subjective improvement in 4 patients and lack of clinical evidence of adverse effects suggested that (153)Sm-EDTMP injection may be an option for the treatment of dogs with MLO or OSA of the skull when other treatments have failed or surgery is not possible.
评估钐Sm 153 依替膦酸((153)Sm-EDTMP)作为患有颅骨骨肿瘤犬的一种治疗选择。
回顾性病例系列。
患有颅骨多叶性骨软骨肉瘤(MLO)或骨肉瘤(OSA)的犬。
检索了密苏里大学和佛罗里达大学1986年至2006年兽医学院教学医院记录中接受(153)Sm-EDTMP治疗的原发性颅骨肿瘤犬。
最初评估了25只犬,5只犬因随访不足或非相关死亡随后被排除。诊断出7例骨肉瘤和13例多叶性骨软骨肉瘤。肿瘤累及枕骨和额骨(n = 10)、颧弓和上颌区域(6)、腭(3)和下颌骨(1)。未记录到与(153)Sm-EDTMP治疗相关的具有临床意义的不良反应。在注射(153)Sm-EDTMP后21天评估的20只犬中,4只主观症状改善,13只病情进展,3只随访不足。根据影像学检查结果,怀疑1只犬发生转移;16只犬未发现明显转移,3只犬的病历资料不足。生存时间定义为从注射(153)Sm-EDTMP之日至死亡之日,范围为3至1314天(中位数,144天)。
4例患者的主观症状改善以及缺乏不良反应的临床证据表明,当其他治疗失败或无法进行手术时,注射(153)Sm-EDTMP可能是治疗患有颅骨MLO或OSA犬的一种选择。